Clinical Research Associate Jobs in France

Precision Medicine Group Clinical Research Team advances oncology and rare disease trials by integrating scientific expertise with innovative data solutions. As a Clinical Research Associate I or II you will monitor study progress at investigative sites, coordinate regulatory submissions, conduct site visits, and ensure compliance with ICH‑GCP and SOPs.

IQVIA Clinical Functional Services Partnerships seeks a Junior Clinical Research Associate to support a single sponsor partner in France. The role involves on-site monitoring, site management, and recruitment tracking for oncology or neurology protocols.

FSO department at Fortrea in Paris focuses on overseeing clinical trial operations to ensure compliance and data integrity. The Senior Clinical Research Associate I monitors trials, conducts site visits, manages site relationships, verifies source documents, and provides investigator training.

IQVIA Clinical Functional Services Partnerships (FSP) team focuses on delivering high‑quality clinical research for a single sponsor, acting as the sponsor’s dedicated partner. The Experienced Clinical Research Associate manages site monitoring across France, drives recruitment plans, trains sites, and mentors junior staff while maintaining risk‑based monitoring practices.

IQVIA Clinical Research team conducts clinical monitoring visits to ensure study integrity and regulatory compliance. The Clinical Research Associate performs site monitoring, protocol training, quality oversight, progress tracking, and documentation while collaborating with study teams.

PSI is a leading Contract Research Organization with over 22 years of industry experience, delivering quality, on-time clinical services across diverse therapeutic indications. As a Clinical Research Associate II in Saint-Maur-des-Fossés, Île-de-France, you will conduct and report onsite monitoring visits, support study startup, perform CRF review and source document verification, manage site communication, and collaborate with internal project teams and vendors.

Clinical Research team at NAMSA conducts global medical device trials ensuring patient safety and regulatory compliance. The Associate monitors sites, conducts qualifications, initiations, interim and close‑out visits, and manages study documentation and metrics.

FSP department at Fortrea France is responsible for overseeing clinical trial operations across France. The Senior Clinical Research Associate II monitors trials, manages site relationships, verifies source documents, and provides investigator training to ensure compliance with ICH GCP and local regulations.

Fortrea Early Careers program welcomes an Intern Clinical Research Associate, FSO to support clinical trial setup, execution, and closure in France. You will liaise with hospital sites, assist regulatory submissions, and collaborate with Clinical Research Associates and Start‑Up Specialists while gaining exposure to trial feasibility and patient recruitment.

Clinical Research Team at AstraZeneca focuses on advancing clinical studies through rigorous monitoring and data management. The intern will be trained on IMPACT, CTMS, RAVE, and eTMF platforms, assist in preparing and conducting site visits (including remote and risk‑based monitoring), and help draft monitoring reports.

Clinical Research Director at Sanofi leads clinical trial strategy for oncology programs. Drives development plans, oversees protocol creation, study execution, and regulatory submissions.

Boston Scientific seeks a Senior Field Clinical Research Engineer to support pre- and post-market cardiac clinical trials across European countries. You will own day-to-day trial execution in your territory, serve as the primary clinical interface for investigators and site staff, and deliver hands-on technical support during EP ablation and cardiac rhythm management procedures in cath lab settings.

Boston Scientific seeks a Senior Field Clinical Research Engineer to support pre- and post-market cardiac clinical trials across European countries. The role involves hands-on technical support during electrophysiology and cardiac rhythm management procedures, site qualification, investigator training, and IRB support, while serving as the primary clinical interface with investigative sites.

Clinical Operations at Merck leads the execution of all clinical trials in France. The role oversees trial quality, regulatory compliance, and budget management while building and leading a high‑performing team across therapy areas.

Global Development organization at Sanofi drives clinical development of R&D programs from early phases through life‑cycle management. The Clinical Research Director leads strategy, protocol design, regulatory submissions and cross‑functional execution to ensure high‑quality data and successful trials.

IQVIA Clinical Research Site in Poitiers focuses on advancing healthcare through rigorous clinical trials. The Clinical Research Coordinator supports the site by maintaining study documentation, screening and enrolling patients, coordinating procedures, and ensuring data quality in electronic capture systems.

Core Surgical Innovations (CSI) at Medtronic drives clinical evidence for innovative medical devices. Senior Clinical Research Specialists design, plan and oversee international pre‑market and post‑market studies, author protocols, manage trial operations and collaborate with cross‑functional teams to ensure regulatory and reimbursement success.

As the Clinical Research Director, you will spearhead cutting‑edge ophthalmic studies, guiding product development through trials, ensuring safety, efficacy, and regulatory compliance to advance eye care.

Clinical Research at Merck leads innovative health solutions through global clinical trials. The Clinical Research Manager Lead oversees a portfolio of trials, drives performance, and mentors a team of managers to ensure quality and compliance.

IQVIA is recruiting a Research Assistant to support a clinical research site in Le Coudray, Paris, France. The part-time role (16 hours per week) involves administrative and clinical support tasks to ensure smooth execution of clinical trials, including maintaining study documentation, supporting patient screening and enrollment, coordinating logistical activities, performing data entry and quality checks, patient education, and communicating with study monitors.